Tag | Content |
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EnhancerAtlas ID | HS187-14784 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:232347330-232348850 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:232347612-232347631 | TGGCCAGCAGGTGGCAGCG | + | 8.24 | STAT3 | MA0144.2 | chr2:232347939-232347950 | CTTCCCAGAAA | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 232347864 | 232348336 | chr2 | 232348515 | 232348679 |
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Enhancer Sequence | GTGCTGGGAT TACTGGCGTG AGCCACCGCA CCCGGCCAGA AAACTCCAAT TCTTAATTCC 60 TTACCTGTAG TGGGGGGTCA TCATCTCTAC CTTACTGATG TAAGGCACAG GACAGTTCAA 120 GAGCGACAGT AACGTGCTGC CACCGTCACT GGGGTGCTGT AGCCGATGTG AACTCCCTCC 180 CCGGCTAGCT TCTCTTCTGT GAAGGTGAGG TCCGGGCCAC CAAGCCGCTT GCCCACTCCA 240 CACAAGGTCC TTCTCTCCGA GGGACGCGGC AGGGGCCCGA GGTGGCCAGC AGGTGGCAGC 300 GCCGCGGCAG CCCGGGTTTG GCATAGCTCG GGAGCGGCCT CCGGGAAAGG AAGGGGTCAG 360 GCCTCTCCAG GCAGCCCCCA GAGCCCCTCG CCTCCCTGGG CGCCCCACTC GCAGATGCAG 420 CAGGGCGGGT TCGCGGGTGT GCGGCCTGCA CCTGGCGGGG CTCCGGGCTT GGGTGGAAGC 480 TCTGCTGTCG CCATCTTGAC GTCTGAGTTA CTGCTGAGCA GGAGCCCTGC ATTTTCATTT 540 TGCGCCAGGC CTCTCAAACT GTGGTCCTGG GTGCCAGGAC TCCTGCTGCC TCGGGATCCC 600 GCCACTTTAC TTCCCAGAAA TGCGCTGAGC CCGTCCCTTT CCTGCCGTTG CTCAGCCTTC 660 CCGGGGCTCC CTGACCATGC TTGTCTCCAG CTCACCGGCC TTCCAGAAGC CTGGAGAGGG 720 CCGGGACCCC ACATGGGGAG GACGAAGAAC CCACGCAAGG AAAACGGGGA CCCTACATGG 780 GCATGGGGCA GCCATGGGGA GGAGGGGGAC CACGTGGGGA TAATGGGGCC ATACGTGGAG 840 AGGAGGGGAC CCTACAGAAG GCCTGGGTTG GGCAGTGCTG GGCTCTCGTC GGAGGGTCAG 900 GTGGCGCTGG CGGCCGGCAG GAAGCCCTGG GTAGCGGGTG GCGGGCAGCA GGTCCCGGGC 960 TGCAGGCCCC GTGGAGAGCG GAAGGCGCGC GGCGAGGCCC GGGCGGGAAC CCAAGGCTGG 1020 AGGCCGGCCC TAAGAGTGCT TCCCTAGCAG CCCCGGCGGG AAAAGAAGAG AACAAAGTCT 1080 AGGAGTTCCG GGACTTCCCC GCGGTGGCAG AGGAGGGGGC TGCCATTGTC AAGGCGGCAC 1140 AGAAGCCTCG GGTTCGGGGA CCTTTGCTGG AGGAGCTGGG GCAGGGTAGG ACGGGGGCCG 1200 CAGGGGCCTC GAGAGCGAAC GGGGAAAGGC CGCGGCGCCT GCAGAGCACA GTCCATGCAG 1260 TTTGCCCGGG GCGCGGGCCT CTCGAGTGTG CTCAGGAAGC CGTGGCTCCT CGGGGCGTCT 1320 GCAGGCCTCC CAGCATCCGT CGTGCAGACC TGACGCCACC TGCCACCCGC AGACGCTGAG 1380 ACCCGGAGCC CCTCTGCCCC TGGGCTGGCC GCGGAGGCTG CCTCTGGGGT GCGGTTTCCC 1440 AGGCTGTGTC TTTTCAGCGG GTGCGCAGGT TCCCGCCCTC CCAGTGTCCC TTCCTGCGGT 1500 CTGGACGTGG GGGCCCGCGG 1520
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